Variant report

Variant	rs11020810
Chromosome Location	chr11:94258375-94258376
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94246000-94267400	Weak transcription	Aorta	Aorta
2	chr11:94246800-94259000	Weak transcription	Stomach Mucosa	stomach
3	chr11:94247200-94258800	Weak transcription	Fetal Intestine Small	intestine
4	chr11:94253400-94258800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:94253600-94258800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr11:94254400-94261800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:94257000-94260800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:94257400-94260600	Enhancers	NHEK	skin
9	chr11:94257400-94262400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:94257800-94259000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:94257800-94260200	Enhancers	HMEC	breast
12	chr11:94258200-94259200	Weak transcription	Placenta	Placenta

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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